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Requirement for the Mitochondrial Pyruvate Carrier in Mammalian Development Revealed by a Hypomorphic Allelic Series

https://doi.org/10.1128/mcb.00166-16
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Taurine Biosynthesis by Neurons and Astrocytes
inferredcites →https://doi.org/10.1074/jbc.m114.566927openalex-snapshot
Mitochondrial Phosphoenolpyruvate Carboxykinase (PEPCK-M) Is a Pro-survival, Endoplasmic Reticulum (ER) Stress Response Gene Involved in Tumor Cell Adaptation to Nutrient Availability
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Carnitine palmitoyltransferase‐1c gain‐of‐function in the brain results in postnatal microencephaly
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A Mitochondrial Pyruvate Carrier Required for Pyruvate Uptake in Yeast, Drosophila , and Humans
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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Metabolite regulation of the mitochondrial calcium uniporter channel
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TATA-Box Binding Protein O-GlcNAcylation at T114 Regulates Formation of the B-TFIID Complex and Is Critical for Metabolic Gene Regulation
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The mitochondrial pyruvate carrier mediates high fat diet-induced increases in hepatic TCA cycle capacity
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Fatty acid oxidation is required for active and quiescent brown adipose tissue maintenance and thermogenic programing
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Tubular mitochondrial pyruvate carrier disruption elicits redox adaptations that protect from acute kidney injury
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